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Elena Gennaro

Showing results (11-20 of 37) with videos related to

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Brain & Development|November 24, 2016
Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathyRobertino Dilena, Pasquale Striano, Elena Gennaro, et al.
BMC Medical Genetics|August 7, 2013
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic settingValentina Gatta, Elena Gennaro, Sara Franchi, et al.
Epilepsy Research|February 2, 2010
Short and long interval cortical inhibition in patients with Unverricht-Lundborg and Lafora body diseaseLaura Canafoglia, Claudia Ciano, Elisa Visani, et al.
Frontiers in Genetics|November 20, 2018
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the <i>FMR1</i> GeneEsperanza Fernández, Elena Gennaro, Filomena Pirozzi, et al.
Brain & Development|October 27, 2009
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patientsFrancesca Ragona, Daniela Brazzo, Ilaria De Giorgi, et al.
Seizure|September 16, 2011
The genetics of monogenic idiopathic epilepsies and epileptic encephalopathiesFrancesco Nicita, Paola De Liso, Federica Rachele Danti, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 30, 2003
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneityElena Gennaro, Pierangelo Veggiotti, Michele Malacarne, et al.
The Journal of Molecular Diagnostics : JMD|November 2, 2013
A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysisMarina Grasso, Elles M J Boon, Stela Filipovic-Sadic, et al.
Epilepsia|December 5, 2012
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutationsLaura Canafoglia, Elena Gennaro, Giuseppe Capovilla, et al.
Biochemical and Biophysical Research Communications|January 25, 2006
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancyElena Gennaro, Filippo M Santorelli, Enrico Bertini, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Brain & Development|November 24, 2016
Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathyRobertino Dilena, Pasquale Striano, Elena Gennaro, et al.
BMC Medical Genetics|August 7, 2013
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic settingValentina Gatta, Elena Gennaro, Sara Franchi, et al.
Epilepsy Research|February 2, 2010
Short and long interval cortical inhibition in patients with Unverricht-Lundborg and Lafora body diseaseLaura Canafoglia, Claudia Ciano, Elisa Visani, et al.
Frontiers in Genetics|November 20, 2018
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the <i>FMR1</i> GeneEsperanza Fernández, Elena Gennaro, Filomena Pirozzi, et al.
Brain & Development|October 27, 2009
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patientsFrancesca Ragona, Daniela Brazzo, Ilaria De Giorgi, et al.
Seizure|September 16, 2011
The genetics of monogenic idiopathic epilepsies and epileptic encephalopathiesFrancesco Nicita, Paola De Liso, Federica Rachele Danti, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 30, 2003
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneityElena Gennaro, Pierangelo Veggiotti, Michele Malacarne, et al.
The Journal of Molecular Diagnostics : JMD|November 2, 2013
A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysisMarina Grasso, Elles M J Boon, Stela Filipovic-Sadic, et al.
Epilepsia|December 5, 2012
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutationsLaura Canafoglia, Elena Gennaro, Giuseppe Capovilla, et al.
Biochemical and Biophysical Research Communications|January 25, 2006
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancyElena Gennaro, Filippo M Santorelli, Enrico Bertini, et al.
Pageof 4